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Rural–urban differentials in 30-day and 1-year mortality following first-ever heart failure hospitalisation in Western Australia: a population-based study using data linkage
  1. Tiew-Hwa Katherine Teng1,
  2. Judith M Katzenellenbogen1,
  3. Joseph Hung2,
  4. Matthew Knuiman3,
  5. Frank M Sanfilippo3,
  6. Elizabeth Geelhoed3,
  7. Michael Hobbs3,
  8. Sandra C Thompson1
  1. 1Western Australian Centre for Rural Health, University of Western Australia, Perth, Western Australia, Australia
  2. 2Sir Charles Gairdner Hospital Unit, School of Medicine and Pharmacology, University of Western Australia, Perth, Western Australia, Australia
  3. 3School of Population Health, University of Western Australia, Perth, Western Australia, Australia
  1. Correspondence to Dr Tiew-Hwa Katherine Teng; katherine.teng{at}uwa.edu.au

Abstract

Objectives We examined differentials in short-term (30-day mortality) and 1-year mortality (in 30-day survivors) following index (first-ever) hospitalisation for heart failure (HF), between rural and metropolitan patients resident in Western Australia.

Design A population-based cohort study.

Setting Hospitalised patients in Western Australia, Australia.

Participants Index patients aged 20–84 years with a first-ever hospitalisation for HF between 2000 and 2009 (with no prior admissions for HF in previous 10 years), identified using the Western Australia linked health data.

Main outcome measures 30-day and 1-year all-cause mortality (in 30-day survivors) following index admission for HF.

Results Of 17 379 index patients with HF identified, 25.9% (4499) were from rural areas. Rural patients were significantly younger at first HF hospitalisation than metropolitan patients. Aboriginal patients comprised 1.9% of metropolitan and 17.2% of rural patients. Despite some statistical differences, the prevalence of antecedents including ischaemic heart disease, hypertension, diabetes and chronic kidney disease was high (>20%) in both subpopulations. After adjusting for age only, patients from rural areas had a higher risk of 30-day death (OR 1.16 (95% CI 1.01 to 1.33)) and 1-year death in 30-day survivors (HR 1.11 (95% CI 1.01 to 1.23)). These relative risk estimates increased and remained significant after further progressive adjustments for Aboriginality, socioeconomic status, insurance status, emergency presentation, individual comorbidities and revascularisation with OR 1.25 (1.06 to 1.48) for 30-day mortality and HR 1.13 (1.02 to 1.27) for 1-year mortality. The addition of the weighted Charlson index to the 30-day model improved the ‘c’ statistic (under the receiver operating characteristic curve) from 0.656 (using a variation of administrative claims model) to 0.714.

Conclusions Remoteness and variable access to healthcare can cause important disparities in health outcomes. Rural patients with HF in Western Australia have poorer risk-adjusted outcomes compared with metropolitan patients. This finding has important implications for chronic disease management and provision of health services in rural Australia.

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Strengths and limitations of this study

  • The strengths of this study lie in the quality and near complete ascertainment of the short-term and long-term mortality after first heart failure (HF) hospitalisation using the Western Australia linked administrative data.

  • A principal diagnosis of HF in the Western Australia linked hospital morbidity data had been previously validated against the Boston diagnostic criteria with a positive predictive value of 92.4% for ‘definite’ HF.

  • We found a higher risk-adjusted 30-day and 1-year mortality (in 30-day survivors) in rural (compared with metropolitan) patients following first HF hospitalisation in Western Australia between 2000 and 2009. The mortality disparity between rural and metropolitan patients persisted after adjustment for Aboriginality, other major sociodemographic differences and comorbidities.

  • However, we do not have information to adjust for medications in our cohort and sociodeprivation was derived using an area-based measure which could give rise to potential misclassification.

  • The findings have implications for enhancing chronic disease management and secondary prevention of HF in rural Western Australia.

Introduction

The management of chronic diseases is an increasing public health concern in rural areas.1 Australians living in regional and remote areas generally have poorer health than metropolitan residents,1 with higher rates of chronic diseases reported in these areas.2 The health needs of many regional and remote communities have not been met,3 despite many initiatives to address geographical inequalities over the last decade. Generally, rural populations experience poorer access to and limited availability of health and allied healthcare services with the provision of healthcare services inversely proportional to the distance from capital cities.1

Rural inhabitants have a constellation of risk factors and experience greater socioeconomic disadvantage4 which also affect people's need for and access to health services.2 Any understanding of the rural dimension in health needs to be inclusive of Indigenous Australians as Aboriginal and Torres Strait Islander peoples are more likely to live in non-metropolitan areas.5 Additionally, cardiovascular disease (CVD), including heart failure (HF), is a major cause of premature death in the indigenous population in Australia.6

HF is a chronic debilitating disease, with 50–60% mortality within 5 years.7 HF is a major cause of death from CVD and outcomes can be adversely affected by restricted access to hospital and continuing care as well as the standard of clinical management.8 Therefore death rates from HF are a useful indicator of disparities in health access and care between rural and metropolitan patients. Previous studies from Canada9 ,10 suggest important disparities in the outcomes of HF among metropolitan versus rural populations. Although Canada has similarities in the universal healthcare system and geography as Australia, there are no previous studies (on HF) in the Australian context.

We examined differentials in 30-day mortality and 1-year mortality (in 30-day survivors) following index (first-ever) hospitalisation for HF, between rural and metropolitan patients resident in Western Australia .

Methodology

Study setting and data sources

The study was performed in Western Australia, which is geographically the largest of six states in Australia, with a land mass spanning 2.53 million km2. Based on the 2006 census, about 27% of the 2.5 million inhabitants in Western Australia lived in what is referred as regional and remote Australia. Western Australia is also home to the third largest number of Aboriginal Australians (13.2% of total Aboriginal population). Australia has a universal healthcare system with free public acute hospital services, while allowing choice through a mix of public and private healthcare service providers.

Data were obtained from the Western Australian Data Linkage System, a population-based electronic linked health database which has been used extensively for health-related research.11 The Hospital Morbidity Data Collection (HMDC), a core dataset of the data linkage system, records information on hospital admissions throughout Western Australia, and is regularly audited for quality and accuracy. HMDC data are routinely linked to the Mortality register using probabilistic matching with greater than 99% accuracy.11

The Emergency Department Data Collection (EDDC) containing data on emergency department (ED) activity in Western Australia's public and private hospitals (under contract with the Western Australian government) was used to examine re-presentations to ED within 1 year of follow-up from index admission of HF.

Ours was a population-based cohort study using linked health data comprising all Western Australian residents aged 20–84 years who were admitted with a first hospitalisation for HF between 2000 and 2009 (with no previous admissions in the past 10 years), as described previously.12 ,13 Inclusion in the study was based on a principal discharge diagnosis of HF or a secondary discharge diagnosis of HF with a principal discharge diagnosis of a cardiovascular condition, excluding acute myocardial infarction (AMI). The coding for HF as a principal discharge diagnosis in the HMDC has been previously validated against the Boston diagnostic criteria with a positive predictive value of 92.4% for ‘definite’ HF.14

Geographical classification

Using residential postcodes, the Accessibility/Remoteness Index of Australia (ARIA) classification was used to define the five categories of residence based on road distance to service centres: major cities, inner regional, outer regional, remote and very remote.15 For the regression analysis, place of residence was dichotomised into metropolitan residence (based on the greater Perth metropolitan city definition,16 including urban and some of inner regional) and rural residence (remainder of inner regional, outer regional, remote and very remote). A sensitivity analysis was performed using three geographical locations: (1) metropolitan,16 (2) regional (remainder of inner regional and all of outer regional) and (3) remote/very remote.

Socioeconomic Indices for Areas (SEIFA)17 were assigned to each patient based on residential postcodes and divided into quintiles, based on predefined cut-off points. The first quintile (Q1) represents the most disadvantaged group and fifth quintile (Q5) the least.

Comorbidities, interventions and procedures

Individual comorbidities within 5 years or concurrent with index HF hospitalisation were identified: hypertension, atrial fibrillation, rheumatic fever and rheumatic heart disease, diabetes, valvular heart disease, chronic kidney disease, renal failure, chronic obstructive pulmonary disease (COPD), unstable angina, AMI, other ischaemic heart disease (IHD) and cerebrovascular disease. A Charlson comorbidity score18 was calculated for each index case by applying a fixed 5-year look-back period using the HMDC. We used the Dartmouth-Manitoba International Classification of Diseases (ICD) code assignments19 in calculating the Charlson score based on the original 17 Charlson comorbidities. Percutaneous coronary intervention or coronary artery bypass grafting and coronary angiography were similarly identified.

Statistical analysis

Descriptive analyses were used to characterise differences in the sociodemographics, comorbidities and interventions/procedures received between patients with HF who reside in metropolitan compared with rural areas. Means and SDs were calculated for continuous variables while frequencies and proportions were derived for categorical data. The Pearson χ2 test was used to test for differences in categorical variables and the t test or Mann-Whitney test for continuous variables. Multivariable logistic regression was used to determine predictors of death within 30 days, with ORs and their 95% CIs reported. Multivariable Cox regression was used to determine survival to 1 year in 30-day survivors and HRs and their 95% CIs reported. All patients admitted between 1 January 2000 and 30 November 2009 were included for 30-day survival analysis. For survival analysis to 1 year (from index admission), only patients admitted with their first HF between 2000 and 2008 were included.

Adjustment for cluster correlation with postcode as the cluster was examined and found to have a non-significant effect and hence not included in the final models.

Results

Table 1 shows the geographic and sociodemographic characteristics of patients with first HF hospitalisation living in metropolitan (n=12 880, 74.1%) and rural areas (n=4499, 25.9%) between 2000 and 2009. A total of 33.6% of rural patients were from remote or very remote areas and the remainder from regional areas. Rural compared with metropolitan patients were significantly younger at first HF hospitalisation (mean age: 68±13 vs 71±12 years, p<0.001), and more likely men (59.3 vs 57.2%, p=0.017). Aboriginal (including Torres Strait Islander) patients comprised 17.2% of rural cases versus 1.9% of metropolitan cases. About 75% of rural patients with HF were seen at public regional or small district hospitals compared with less than 1% of metropolitan patients. Rural patients were less likely to have private health insurance compared with metropolitan patients (20.3% vs 32.6%, p<0.001). More than 50% of rural patients (vs 13.4% metropolitan patients) were in the two lowest quintiles (index of most disadvantages) of SEIFA, a proxy for socioeconomic status.

Table 1

Baseline characteristics and crude mortality of metropolitan versus rural patients with a ‘first-ever’ (index) admission for heart failure between 2000 and 2009

Profile of care prior to the index hospitalisation for HF and prehospital emergency medical service (EMS) coverage by ambulance was different in both subpopulations (table 1). Metropolitan (vs rural) patients were more likely to be managed by specialist clinicians (25.2% vs 15.1% rural); by contrast, more rural patients were cared for by general practitioners (18.4% vs 4.9% metropolitan). Metropolitan (vs rural) patients were more likely to be transported by EMS ambulance to admitting hospitals (38.5% vs 19.4%). About 65% of rural patients depended on private/public transport to get to admitting hospitals. Notably, rural (vs metropolitan) patients were also more likely (49.1% vs 20.4%) to present to EDs (for any condition) with triage scores of 4 or 5 (for semiurgent or non-urgent cases) during the 1-year follow-up, suggesting EDs being used to fill the gaps in primary care or specialist services in rural areas.

A higher proportion of rural patients had a Charlson index of 1–2 although a small but significantly larger proportion of metropolitan patients (being older) scored >3 (table 1). Despite some statistical differences between metropolitan and rural patients, there was a high prevalence of potential antecedent HF risk factors including IHD, hypertension, atrial fibrillation, diabetes, chronic kidney disease, COPD, cerebrovascular disease and rheumatic and non-rheumatic valvular heart disease in both subpopulations (see table 1). Rates of coronary interventions (prior to or on index admissions) were low overall but significantly lower in rural patients. When adjusted for age, sex, period, Aboriginality and Charlson comorbidity index, rural patients with HF were less likely to have coronary angiography compared with metropolitan patients (risk-adjusted OR=0.81 (95% CI 0.77 to 0.86, p<0.001)).

Crude 30-day and 1-year cumulative all-cause mortality and unadjusted risk were not significantly different between metropolitan and rural patients with first HF hospitalisation (tables 1 and 2). After age adjustment only, patients from rural areas had a higher risk of 30-day death (OR 1.16 (95% CI 1.01 to 1.33)) and 1-year death in 30-day survivors (HR 1.11 (95% CI 1.01 to 1.23), see table 2). The difference in survival between rural and metropolitan patients increased with further adjustment for sociodemographic differences including Aboriginality, SEIFA (as proxy for socioeconomic status), private insurance status, emergency presentation and the Charlson comorbidity index, with OR of 1.26 and HR of 1.14. The association between rurality and mortality persisted between the two subpopulations after further adjustment to include other individual comorbidities of interest, significant interaction effects and interventions (see table 2). The addition of the weighted Charlson index to the 30-day model (using a variation of the administrative claims model)20 improved the ‘c’ statistic (under the receiver operating characteristic curve) from 0.656 to 0.714.

Table 2

Step-wise risk adjustment for 30-day and 1-year mortality (in 30-day survivors) in rural patients with index heart failure versus metropolitan patients

No significant interactions were found between sex and rurality, and Aboriginality and rurality (as location of residence). Further evaluation of mortality in men and women separately and in younger (<55 years) and older patients showed similar ORs/HRs of death at 30 days and 1 year (in 30-day survivors) in rural patients compared with metropolitan patients.

A sensitivity analysis using three levels of geographical residence (metropolitan, regional and remote) indicates that regional patients had significantly higher adjusted 30-day and 1-year mortality (in 30-day survivors) than metropolitan patients (table 3). However, the slightly higher OR for 30-day mortality in remote patients (1.29; 95% CI 0.98 to 1.69) did not reach significance in the fully adjusted model, and the adjusted HR for 1-year mortality (in 30-day survivors) was not higher in remote patients (table 3).

Table 3

Sensitivity analysis showing step-wise risk adjustment for 30-day and 1-year mortality (in 30-day survivors) in patients with index heart failure by level of residential location

Discussion

HF is a complex, disabling and potentially deadly clinical syndrome, of increasing public health importance as the population ages.21 Our study examined hospitalised patients with ‘first-ever’ HF, and accordingly, a vast majority (>93%) were emergency presentations to hospital. In this population-based cohort of patients, we found that a sizeable minority of patients (26%) live in rural/remote Western Australia. The majority of the rural patients with HF were from areas of social disadvantage with limited or no access to specialist services for HF, as others have found.22 ,23 Rural area of residence was consistently associated with higher risk-adjusted OR and HR of short-term mortality at 30 days and 1 year (in 30-day survivors) respectively, compared with metropolitan patients, even after controlling for socioeconomic status, Aboriginality, private insurance status and risk factors. The same findings were observed in the subgroup analyses: men and women who lived in rural/remote areas of Western Australia, as well as in older patients aged 55 years and over.

Earlier research by Clark et al24 showed a significantly higher prevalence of congestive HF in rural compared with metropolitan areas among patients aged 60 years and over. Furthermore, rates of echocardiography for diagnosis or specialist referrals and rate of prescribing ACE inhibitor drugs were consistently lower in rural compared with metropolitan areas.24 Different pharmacotherapy patterns in rural and metropolitan Canadian patients with HF have also been reported.9 We found that receipt of coronary angiography or interventions were lower in rural patients, consistent with the previous findings,10 ,24 although disparity in discharge medications was not examined in our study.

Western Australia is geographically large, being the size of Western Europe, with much of its area sparsely populated. Accordingly, the tyranny of distance and lack of transport (as the interface between different entry points to the healthcare system) are major obstacles to accessing appropriate healthcare for rural West Australians. Access to appropriate specialist expertise also requires transfer between services and there are many reasons why such transfers may not occur. Moreover, there may be limited access to comprehensive primary healthcare services, poor integration between different levels of care and inadequate services to support ongoing home-based intervention and HF self-management,25 HF-specific cardiac rehabilitation programmes26 and socioculturally appropriate services.27–29 Hence, the dimension of metro–rural divide in the context of Western Australia is larger than that which occurs in other states.30 Issues of rural and remote health are much more complex than merely the practice of health in another location3 and are affected by issues such as workforce shortages and retention of healthcare workers, higher out-of-pocket costs and the time and cost of travel.3

Rural and remote patients with HF differed considerably from metropolitan patients including being younger, more socially disadvantaged and more likely to be Aboriginal. Despite Australia having universal health insurance through Medicare which allows free access to public hospital treatment and outpatient medical consultations and medications being subsidised, there remain barriers to specialist consultations for socially disadvantaged groups, particularly where upfront cash payments are required. An even more important disparity is the paucity of specialist cardiology care in regional/remote areas. This is evident from the differences in profiles of care between the two subpopulations and the findings that showed rural patients were utilising EDs to fill the gaps in the primary healthcare and the specialist services in rural areas. Other evidence shows that increasing private health insurance coverage in Australia has been associated with loss of equity after controlling for other factors.30 ,31

The heterogeneity in the different geographical areas needs to be highlighted. However, our results showed that despite further adjustments for demographics, SEIFA and private health insurance status (both as a proxy for socioeconomic status), Aboriginality, emergency presentations, individual comorbidities and interventions, differential difference in mortality outcomes persisted for rural patients compared with metropolitan patients. It is plausible that the type of care received from regional, small district hospitals and/or rural primary care providers compared with metropolitan hospitals and urban general practices has a differential impact on mortality. Around 75% of the rural patients were managed at regional, small district hospitals, while a vast majority of urban patients were treated in tertiary and private hospitals. There might be another reason why fewer people have private insurance in rural areas—because there are only two private hospitals in rural areas, and going in as a private patient in a public rural hospital offers little advantage. Hence, rural residents may not see a need for private insurance, and they probably think the likelihood of being admitted to a metro private hospital is low.

In the sensitivity analysis with the three levels for residential location, regional patients showed increased risk-adjusted ORs/HRs of 30-day and 1-year mortality (in 30-day survivors). The association for remote/very remote patients was marginally significant (for 30-day mortality) possibly because of a lack of power. However, previous work by Katzenellenbogen et al32 found that some older groups living in remote areas had lower MI rates than metropolitan residents, suggesting a possible migration effect of remote patients with heart disease moving to regional/metro centres. The data from the current study may reflect such a phenomenon, with remote patients with HF moving to more accessible centres after their incident event and thus benefiting through improved 1-year survival.

Our results are consistent with other studies from Canada and the USA which also reported worse outcomes in rural versus metropolitan patients with HF.8–10 The same rural–metropolitan differential in Western Australia was reported for the incidence of MI in Western Australia.32 However, conflicting evidence was reported from a CVD risk study on South-West Victoria and North-West Adelaide, Australia.30 That study examined cardiovascular mortality rates without comprehensive adjustment and only a small proportion of the patients examined were Aboriginal.30 There is also a contextual difference in that HF has high mortality with patients often presenting with heavy comorbidity burden.

The problem of inequalities in health burden and access to healthcare related to rurality and remoteness is a common theme across many countries including high socioeconomic countries such as Australia and Canada. It is therefore an important issue that is relevant to health policy, health service delivery and healthcare planning in many countries beyond the local context.

The strengths of this study lie in the quality and near complete ascertainment of the short-term and long-term mortality after first HF hospitalisation using linked administrative data in Western Australia,11 and the previous validation with respect to a principal diagnosis of HF.14 However, sociodeprivation was derived using an area-based measure which gives rise to potential misclassification at an individual level. We have no information as to why people choose not to have private health insurance. Our study also lacked information on use of medications in our cohort. However, in a separate study undertaken by our team,33 the authors found adjusted evidence-based prescription at discharge for patients with acute coronary syndrome was significantly lower in district hospitals versus metropolitan teaching hospitals (OR 0.51 (95% CI 0.32 to 0.82)), as well also in patients with regional versus metropolitan residence (OR 0.55 (95% CI 0.39 to 0.77)). This finding is also likely applicable to the uptake and adherence to evidence-based therapy for patients with HF discharged from non-tertiary and rural care hospitals. We have previously shown that the discharge prescription of evidence-based HF medications had a significant impact on subsequent survival.34

Conclusions

This study highlights the impact of geographical or spatial isolation on mortality outcomes in patients with HF as the first step in understanding rural–urban differences. From the health policy perspective, the higher rural mortality likely points to the inequalities in the availability and access to appropriate medical care, rather than compositional differences in rural and metropolitan patients with HF. Rural Western Australia is not homogeneous and the proportion of Aboriginal people increases with remoteness. This has implications for the provision of collaborative models of care for chronic disease management and secondary prevention of HF in rural areas.

Acknowledgments

The authors thank the Western Australian Data Linkage Branch and the staff of the Inpatient Data Collections for the provision of the data and the Registry of Births, Deaths and Marriages for providing the death data.

References

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Footnotes

  • Contributors All authors critically reviewed and contributed to the intellectual content of the manuscript. T-HKT, JMK, MK, SCT and JH were involved with the conception of the study. T-HKT performed the statistical analyses, supported by MK and drafted the manuscript. SCT, JH and MH provided the clinical expertise. All authors have read and approved the final version of the manuscript.

  • Funding The study had been supported by the National Health and Medical Research Council (NHMRC) project grant (#1031057). The Western Australian Centre for Rural Health receives funding from the Department of Health and Ageing. JMK is funded by an NHMRC Early Career Fellowship (#037429).

  • Competing interests None.

  • Ethics approval The Western Australia Aboriginal Health Ethics Committee and Human Research Ethics Committees of the Department of Health Western Australia and The University of Western Australia.

  • Provenance and peer review Not commissioned; externally peer reviewed.

  • Data sharing statement No additional data are available. Data provided by the Western Australian Department of Health, via the Data Linkage Branch. Linked personal health information is confidential and cannot be shared. The investigators and institution are bound by confidentiality agreements which prevent complying with this Data Sharing Policy.

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